| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 191801 | BAA02g26570 | A02 | 14849343 | C | T | synonymous_variant | LOW | c.330G>A|p.Ser110Ser |
S182 S70 |
| 191802 | BAA02g26570 | A02 | 14849588 | C | T | missense_variant | MODERATE | c.85G>A|p.Gly29Arg |
S237 |
| 191803 | BAA02g26570 | A02 | 14850864 | G | A | upstream_gene_variant | MODIFIER | c.-1192C>T| |
S127 |
| 191804 | BAA02g26570 | A02 | 14851665 | G | A | upstream_gene_variant | MODIFIER | c.-1993C>T| |
S174 S216 S27 |
| 191805 | BAA02g26570 | A02 | 14852515 | C | T | upstream_gene_variant | MODIFIER | c.-2843G>A| |
S142 |
| 191806 | BAA02g26570 | A02 | 14853094 | G | A | upstream_gene_variant | MODIFIER | c.-3422C>T| |
S280 |
| 191807 | BAA02g26580 | A02 | 14855399 | G | A | downstream_gene_variant | MODIFIER | c.*444C>T| |
S263 |
| 191808 | BAA02g26580 | A02 | 14855663 | C | T | downstream_gene_variant | MODIFIER | c.*180G>A| |
S164 |
| 191809 | BAA02g26580 | A02 | 14856622 | C | T | upstream_gene_variant | MODIFIER | c.-435G>A| |
S270 |
| 191810 | BAA02g26580 | A02 | 14859025 | G | A | upstream_gene_variant | MODIFIER | c.-2838C>T| |
S280 |
| 191811 | BAA02g26580 | A02 | 14860839 | G | A | upstream_gene_variant | MODIFIER | c.-4652C>T| |
S197 |
| 191812 | BAA02g26590 | A02 | 14863502 | C | T | downstream_gene_variant | MODIFIER | c.*1227G>A| |
S206 |
| 191813 | BAA02g26590 | A02 | 14863597 | G | A | downstream_gene_variant | MODIFIER | c.*1132C>T| |
S278 |
| 191814 | BAA02g26590 | A02 | 14863801 | G | A | downstream_gene_variant | MODIFIER | c.*928C>T| |
S71 |
| 191815 | BAA02g26590 | A02 | 14863849 | C | T | downstream_gene_variant | MODIFIER | c.*880G>A| |
S49 |
| 191816 | BAA02g26590 | A02 | 14864042 | G | A | downstream_gene_variant | MODIFIER | c.*687C>T| |
S200 |
| 191817 | BAA02g26590 | A02 | 14864952 | C | T | missense_variant | MODERATE | c.1541G>A|p.Gly514Glu |
S267 |
| 191818 | BAA02g26590 | A02 | 14865191 | C | T | synonymous_variant | LOW | c.1302G>A|p.Gln434Gln |
S105 S106 |
| 191819 | BAA02g26590 | A02 | 14865897 | G | A | missense_variant | MODERATE | c.596C>T|p.Pro199Leu |
S125 |
| 191820 | BAA02g26590 | A02 | 14865989 | G | A | synonymous_variant | LOW | c.504C>T|p.Val168Val |
S68 |
| 191821 | BAA02g26590 | A02 | 14867630 | G | A | upstream_gene_variant | MODIFIER | c.-1138C>T| |
S174 S27 |
| 191822 | BAA02g26590 | A02 | 14868726 | G | A | upstream_gene_variant | MODIFIER | c.-2234C>T| |
S172 S202 |
| 191823 | BAA02g26590 | A02 | 14870348 | G | A | upstream_gene_variant | MODIFIER | c.-3856C>T| |
S35 |
| 191824 | BAA02g26590-BAA02g26600 | A02 | 14871561 | C | T | intergenic_region | MODIFIER | n.14871561C>T| |
S2 |
| 191825 | BAA02g26590-BAA02g26600 | A02 | 14871666 | C | T | intergenic_region | MODIFIER | n.14871666C>T| |
S268 |